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Ifs 55 ft ir spectrometer

Manufactured by Bruker
Sourced in Switzerland

The IFS 55 FT-IR spectrometer is a Fourier-transform infrared (FT-IR) spectrometer manufactured by Bruker. The core function of the IFS 55 is to measure and analyze the infrared absorption spectrum of samples, providing information about their molecular composition and structure.

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4 protocols using ifs 55 ft ir spectrometer

1

Potassium Bromide FTIR Spectroscopy

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Fourier-transform infrared spectroscopy (FTIR) spectra were obtained by the potassium bromide disc technique using an IFS 55 FT-IR spectrometer (Bruker Ltd., MA, Switzerland). Each sample was scanned from 4000 to 400 cm−1 and resolution was taken as 4 cm−1.
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2

FT-IR Analysis of Drug-Loaded Nanoparticles

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FT-IR spectra of the FA conjugated CS, crude gefitinib, P407/PLGA NPs, physical mixture of gefitinib and P407/PLGA NPs, GFB/FCPP NPs, and GFB/FCPP-NEMs were recorded using a Bruker IFS 55 FT-IR spectrometer (Bruker Optics GmbH, Ettlingen, Germany). Before measurement, each sample was ground and pressed into potassium bromide discs.
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3

FTIR Analysis of NAR and F127 Interaction

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The interaction between NAR and F127 was analyzed by FTIR using the Bruker IFS 55 FTIR spectrometer (Bruker Ltd., Switzerland) in the 4000–500 cm−1 wavelength range with a resolution of 2 cm−1 scannings. The samples were compressed into tablets with potassium bromide.
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4

Physicochemical Characterization of OEA-SPC Nanoparticles

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The OEA–SPC NPs was analysed using XRD (Phillips X’pert Pro Super), FTIR (Bruker IFS-55 FTIR spectrometer), and H1NMR (AVANCE III 600 MHz). The bulk OEA powers, SPC, and the physical mixture of OEA and SPC were used as control. Morphology of the OEA–SPC NPs was examined by SEM (UV-70) and TEM (JEM-2100) at 5 and 200 kV, respectively. The Size and zeta-potential values were determined by a Malvern Zetasizer Nano-ZS machine (Malvern Instruments, Malvern). Three parallel measurements were carried out to determine the average values. The content of OEA in OEA–SPC NPs was determined by LC–MS (3200Qtrap). The content efficiency was calculated by Eq. (1): Drug loading content of OEA%=(weight of OEA in NPs)/(weight of NPs)×100%
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